CCD™ Spinal System

GUDID 00673978108513

SCREW C3074L50 CDH CNICAL SAC BLOCK 7X50

MEDTRONIC SOFAMOR DANEK, INC.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00673978108513
NIH Device Record Key61208518-1218-4fc3-980f-bb0aaebecd1a
Commercial Distribution StatusIn Commercial Distribution
Brand NameCCD™ Spinal System
Version Model NumberC3074L50
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter
Length50 Millimeter
Outer Diameter7 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100673978108513 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWPAPPLIANCE, FIXATION, SPINAL INTERLAMINAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


[00673978108513]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-08-24

On-Brand Devices [CCD™ Spinal System]

00673978111551SCREW C8100T CCD TI MIO PLUG
00673978111544SCREW C8100KT CCD TI M10 PLUG KOREA
00673978108599SCREW C3074L70 CDH CNICL SAC BLOCK 7X70
00673978108551SCREW C3074L60 CDH CNICL SAC BLOCK 7X60
00673978108537SCREW C3074L55 CDH CNICL SAC BLOCK 7X55
00673978108513SCREW C3074L50 CDH CNICAL SAC BLOCK 7X50
00673978108490SCREW C3074L45 CDH CNICL SAC BLOCK 7X45
00673978108476SCREW C3074L40 CDH CNICL SAC BLOCK 7X40
00673978108452SCREW C3074L35 CDH CNICL SAC BLOCK 7X35

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